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bioRxiv · 10.1101/2020.12.15.422853

Oncogene-induced cardiac neoplasia shares similar mechanisms with heart regeneration in zebrafish

Pfefferli, C.·Bonvin, M.·Robatel, S.·Perler, J.·Koenig, D.·Jazwinska, A.
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Abstract

The human heart is a poorly regenerative organ and cardiac tumors are extremely rare. The zebrafish heart can restore its damaged myocardium through cardiomyocyte proliferation. Whether this endogenous capacity causes a susceptibility to neoplasia remains unknown. Here, we established a strategy to conditionally express the HRASG12V oncogene in zebrafish cardiomyocytes. The induction of this transgene in larvae or adult animals resulted in heart overgrowth with abnormal histology. The malformed ventricle displayed similar characteristics to the regenerative myocardium, such as enhanced cell-cycle entry, incomplete differentiation, reactivation of cardiac embryonic programs, expression of regeneration genes, oxidative metabolism changes, intramyocardial matrix remodeling and leucocyte recruitment. We found that oncogene-mediated cardiac tumorigenesis and cryoinjury-induced regeneration involve TOR signaling, as visualized by phosphorylation of its target ribosomal protein S6. The inhibition of TOR by rapamycin impaired regeneration and rescued from neoplasia. These findings demonstrate the existence of common mechanisms underlying the proliferative plasticity of zebrafish cardiomyocytes during advantageous organ restoration and detrimental tumorigenesis.

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Pfefferli, C., Bonvin, M., Robatel, S., Perler, J., Koenig, D., Jazwinska, A.. 2020-12-15. Oncogene-induced cardiac neoplasia shares similar mechanisms with heart regeneration in zebrafish. https://doi.org/10.1101/2020.12.15.422853

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